Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3326212015 | Hyperuricemia, anemia, renal failure syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326213013 | Hyperuricemia, anemia, renal failure syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326214019 | Hyperuricaemia, anaemia, renal failure syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326215018 | Familial juvenile hyperuricemic nephropathy type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326216017 | Familial juvenile hyperuricaemic nephropathy type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326217014 | Renin associated familial juvenile hyperuricemic nephropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326218016 | Renin associated familial juvenile hyperuricaemic nephropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3326219012 | A rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3326220018 | A rare autosomal dominantly inherited disease of childhood characterised by hypoproliferative anaemia, hyperuricaemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hyperuricemia, anemia, renal failure syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hyperuricemia, anemia, renal failure syndrome (disorder) | Is a | Hyperuricemia | true | Inferred relationship | Some | ||
Hyperuricemia, anemia, renal failure syndrome (disorder) | Is a | Renal tubular disorder | true | Inferred relationship | Some | ||
Hyperuricemia, anemia, renal failure syndrome (disorder) | Is a | Urate nephropathy | true | Inferred relationship | Some | ||
Hyperuricemia, anemia, renal failure syndrome (disorder) | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
Hyperuricemia, anemia, renal failure syndrome (disorder) | Finding site | Renal tubule structure (body structure) | true | Inferred relationship | Some | 1 | |
Hyperuricemia, anemia, renal failure syndrome (disorder) | Finding site | Kidney structure | false | Inferred relationship | Some | 2 | |
Hyperuricemia, anemia, renal failure syndrome (disorder) | Causative agent | Urate | false | Inferred relationship | Some | 2 | |
Hyperuricemia, anemia, renal failure syndrome (disorder) | Causative agent | Urate | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets